510(k) K992232 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
FIRST RESPONSE 1-STEP PREGNANCY
| Applicant | Armkel, LLC, Cranbury NJ, US |
| Decision | Substantially Equivalent, Dec 21, 1999 |
| Received | Jul 2, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992232
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.